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Ask your administrator if you think this is wrong. ======= MYBBP1A ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: MYBBP1A * **<color #00a2e8>Official Name</color>**: MYB binding protein 1a * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=10514|10514]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q9BQG0|Q9BQG0]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=MYBBP1A&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20MYBBP1A|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/604885|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: This gene encodes a nucleolar transcriptional regulator that was first identified by its ability to bind specifically to the Myb proto-oncogene protein. The encoded protein is thought to play a role in many cellular processes including response to nucleolar stress, tumor suppression and synthesis of ribosomal DNA. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]. * **<color #00a2e8>UniProt Summary</color>**: May activate or repress transcription via interactions with sequence specific DNA-binding proteins. Repression may be mediated at least in part by histone deacetylase activity (HDAC activity). Acts as a corepressor and in concert with CRY1, represses the transcription of the core circadian clock component PER2. Preferentially binds to dimethylated histone H3 'Lys-9' (H3K9me2) on the PER2 promoter. {ECO:0000250|UniProtKB:Q7TPV4}. <button type='primary' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> |DNA pol phi| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |NLS-dependent protein nuclear import complex| |positive regulation of anoikis| |regulation of anoikis| |cellular response to glucose starvation| |intrinsic apoptotic signaling pathway by p53 class mediator| |E-box binding| |circadian regulation of gene expression| |positive regulation of gene expression, epigenetic| |positive regulation of cell cycle arrest| |regulation of cell cycle arrest| |respiratory electron transport chain| |signal transduction by p53 class mediator| |osteoblast differentiation| |circadian rhythm| |intrinsic apoptotic signaling pathway| |cellular response to starvation| |cellular respiration| |electron transport chain| |response to starvation| |cellular response to nutrient levels| |energy derivation by oxidation of organic compounds| |regulation of gene expression, epigenetic| |transcription corepressor activity| |ossification| |cellular response to extracellular stimulus| |rhythmic process| |apoptotic signaling pathway| |positive regulation of cell cycle process| |ribosome biogenesis| |transcription factor binding| |cellular response to external stimulus| |positive regulation of cell cycle| |sequence-specific DNA binding| |generation of precursor metabolites and energy| |ribonucleoprotein complex biogenesis| |response to nutrient levels| |response to extracellular stimulus| |positive regulation of apoptotic process| |positive regulation of programmed cell death| |intracellular membrane-bounded organelle| |positive regulation of cell death| |regulation of cell cycle process| |nucleolus| |apoptotic process| |oxidation-reduction process| |programmed cell death| |cell death| |regulation of cell cycle| |negative regulation of transcription, DNA-templated| |negative regulation of nucleic acid-templated transcription| |negative regulation of RNA biosynthetic process| |negative regulation of RNA metabolic process| |negative regulation of cellular macromolecule biosynthetic process| |RNA binding| |negative regulation of nucleobase-containing compound metabolic process| |negative regulation of macromolecule biosynthetic process| |negative regulation of cellular biosynthetic process| |regulation of apoptotic process| |negative regulation of biosynthetic process| |regulation of programmed cell death| |regulation of cell death| |intracellular signal transduction| |cellular response to stress| |negative regulation of gene expression| |positive regulation of gene expression| |membrane| </modal> \\ === CRISPR Data === <button type='default' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> No hits were found. </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> Global Fraction of Cell Lines Where Essential: 143/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|5/28| |blood|7/28| |bone|2/26| |breast|4/33| |central nervous system|5/56| |cervix|0/4| |colorectal|5/17| |esophagus|4/13| |fibroblast|0/1| |gastric|1/16| |kidney|9/21| |liver|4/20| |lung|12/75| |lymphocyte|2/16| |ovary|8/26| |pancreas|9/24| |peripheral nervous system|4/16| |plasma cell|2/15| |prostate|0/1| |skin|3/24| |soft tissue|2/9| |thyroid|0/2| |upper aerodigestive|5/22| |urinary tract|11/29| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 1261 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 7.68 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='MYBBP1A Expression in NALM6 Cells: 7.68'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2025/12/10 20:19by 127.0.0.1